| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335621-46335797 | Common:5; Rare:80; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762476-46762669 | Common:3; Rare:73 | ||||
| chr22:50185690-50185942 | Common:4; Rare:106 | ||||
| chr22:50244991-50245070 | Rare:32 | ||||
| chr22:50582818-50583121 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628052-50628282 | Common:9; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783606-50783859 | Common:2; Rare:75 | ||||
| chr3:3126792-3126984 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr3:4493177-4493348 | Rare:60 | ||||
| chr3:8501644-8501928 | Common:2; Rare:104 | ||||
| chr3:9363018-9363127 | Rare:39 | ||||
| chr3:9397437-9397693 | Common:1; Rare:94 | ||||
| chr3:9749818-9750007 | Rare:63 | ||||
| chr3:9792364-9792583 | Rare:63 | ||||
| chr3:9792767-9793124 | Common:3; Rare:122 |